Evidence map›Paper›PMID 42524383›Full record

ArticleInternational journal of medical sciences2026

C1q CIC in Lupus Nephritis: An Analysis of 883 Patients.

Huang-Chen Chang, Yen-Ching Wu, Jun-Peng Chen, Wen-Nan Huang, Yi-Hsing Chen, Yi-Ming Chen

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Article in International journal of medical sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Huang-Chen ChangDivision of Allergy, Immunology and Rheumatology, Taichung Veterans General Hospital, Taichung, Taiwan.
Yen-Ching WuDivision of Allergy, Immunology and Rheumatology, Taichung Veterans General Hospital, Taichung, Taiwan.
Jun-Peng ChenDepartment of Medical Research, Taichung Veterans General Hospital, Taichung, Taiwan.
Wen-Nan HuangDivision of Allergy, Immunology and Rheumatology, Taichung Veterans General Hospital, Taichung, Taiwan.
Yi-Hsing ChenDivision of Allergy, Immunology and Rheumatology, Taichung Veterans General Hospital, Taichung, Taiwan.
Yi-Ming ChenDivision of Allergy, Immunology and Rheumatology, Taichung Veterans General Hospital, Taichung, Taiwan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Lupus nephritis (LN) is a major complication of systemic lupus erythematosus (SLE). This study evaluated the association of C1q-circulating immune complexes (C1q CIC) with LN and their potential adjunctive rule-out value compared with conventional biomarkers. Methods: We conducted a retrospective analysis of 883 SLE patients from the Asia Pacific Lupus Collaboration (APLC) cohort in Taiwan. C1q CIC was assessed for its association with disease activity and compared to anti-dsDNA, C3, and C4. Logistic regression and ROC analysis were performed. Results: C1q CIC levels were significantly elevated in active SLE and in non-renal manifestations, including cutaneous involvement, serositis, and hematologic abnormalities. In patients with LN, C1q CIC levels were significantly higher than in those without LN, whereas anti-dsDNA, C3, and C4 showed no significant differences. Overall discriminative performance was modest, and C1q CIC is not suitable as a diagnostic or screening tool for LN. At a cutoff of 5.31 μg Eq/mL, C1q CIC showed a high negative predictive value (NPV = 86.04%) but low positive predictive value (PPV = 29.51%). In stratified analysis, discriminative ability was limited in patients with low disease activity (SLEDAI-2K < 4; AUC = 0.55), whereas NPV remained high (97.15%). Conclusion: C1q CIC may serve as an adjunctive rule-out biomarker for LN, particularly when levels are low or in patients with low disease activity. Although not suitable for diagnosis or screening, its relatively high NPV may help identify patients at lower risk of LN. Results should be interpreted in conjunction with clinical and laboratory assessment.

Indexed as

Complement C1qLupus Erythematosus, SystemicLupus NephritisAdultAntibodies, AntinuclearBiomarkersComplement C3Complement C4FemaleHumansMaleMiddle AgedRetrospective StudiesTaiwanAntibodies, AntinuclearBiomarkersComplement C1qComplement C3Complement C4C1q CIClupus nephritisrule-out biomarkersystemic lupus erythematosus

Identifiers

PMID42524383
PMCPMC13411602

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.